Canonical Allele Identifier: CA435644229
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129249873C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531030C>A , CM000665.2:g.129531030C>A GRCh38
NC_000003.11:g.129249873C>A , CM000665.1:g.129249873C>A GRCh37
NC_000003.10:g.130732563C>A NCBI36
NG_009115.1:g.7392C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.516C>A MANE Select ENSP00000296271.3:p.Leu172=
ENST00000296271.3:c.516C>A ENSP00000296271.3:p.Leu172=
NM_000539.3:c.516C>A MANE Select NP_000530.1:p.Leu172=
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